classifications of thyroid tumours

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    CLASSIFICATION OF THYROID

    TUMORS

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    THYROID TUMORS

    BENIGN MALIGNANT

    PRIMARY SECONDARY

    IFFERNTIATED UNDIFFERENTIATED PARAFOLLICULAR LYMPHOID

    FOLLICULAR

    PAPILLARY

    ANAPLASTIC MEDULLARY LYMPHOMA

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    THYROID TUMORS

    BENIGN MALIGNANTFOLLICULAR ADENOMA

    PRIMARY SECONDARY

    DIFFERENTIATED METASTASIS

    - FOLLICULAR

    - PAPILLARY

    UNDIFFERENTIATED

    - ANAPLASTIC

    PARAFOLLICULAR

    - MEDULLARYLYMPHOID CELL

    - LYMPHOMA

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    FOLLICULAR ADENOMA

    - Presents as a solitary nodule

    - Seen approx in 1% population

    - It is characterised by 4 features

    - Solitary nodule- Complete encapsulation

    - Clearly distinct architecture

    - Compression of the thyroid parenchyma

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    PAPILLARY CARCINOMA

    - It is a most common type of thyroidcarcinoma

    - Comprises of 70-80%

    - Slow growing malignant tumor- It presents as a asymptomatic solidary nodule

    - Involvement of regional lymph nodes

    common.

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    PAPILLARY CARCINOMA

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    FOLLICULAR CARCINOMA

    - It comprises of 10-12%- Common in females

    - It can occur denovo or in a pre-existing multi

    nodular goitre.- It presents either as a solitary nodule or

    irregular firm & nodular thyroid enlargement.

    - Blood borne metastasis is more common.

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    FOLLICULAR CARCINOMA

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    MEDULLARY CARCINOMA

    - It is less frequent (5%)- It arises from the parafollicular cells

    - There are 3 distinctive features

    - Familial occurance

    - Secretion of calcitonin

    - Amyloid stroma

    - Regional lymph node metastasis may occur.

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    MEDULLARY CARCINOMA

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    ANAPLASTIC CARCINOMA

    - It comprises of

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    MALIGNANT LYMPHOMA

    - It is NHL type.- Occurs in pre-existing Hashimotos

    Thyroiditis.

    - Chemotherapy is the main treatment.

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    PAPI LLARY FOLL ICULAR ANAPLASTIC MEDULLARY

    AETIOLOGY Irradiation Endemic

    goitre

    Unknown Sporadic or

    familiar

    INCIDENCE 60% 17% 13% 6%

    AGE 20-40yrs 30-50yrs >50yrs Middle age

    DIAGNOSIS Thyroid

    swelling with

    lymph nodes

    Swelling,meta

    stasis

    Swelling,local

    invasion

    Difficult to

    diagnose

    clinically

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    MICROSCOPY Orphan annie-

    eyed

    nuclei,psommo

    ma bodies

    Angio &

    capsular

    invasion

    Poorly

    differentiated

    cells

    Amyloid

    stroma like

    carcinoid

    SPREAD Lymphatic blood Local

    infiltration

    Lymphatic,b

    lood

    INVESTIGATION

    FNAC Frozensection

    FNAC,biopsy FNAC,calcitonin

    TREATMENT

    OF PRIMARY

    Near total

    thyroidectomy

    Near total

    thyriodecto

    my

    Isthmusectom

    y,external RT

    Total

    thyroidecto

    my

    TREATMENT

    OF

    METASTASIS

    Functional

    block

    dissection

    Radio-

    iodine I131

    or external

    RT

    Palliativa

    external

    radiotherapy

    RBD

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    THANK YOU